2-(Bromoacetyl)thiophene TCI B5383

Chemical Identity

CAS No.: 10531-41-6
PubChem: CID 2776372·SID 468590587
Formula: C6H5BrOS
Molecular weight: 205.07 g/mol
Purity: >95.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromo-1-thiophen-2-ylethanone
SMILES: C1=CSC(=C1)C(=O)CBr
InChIKey: UHWNENCHFSDZQP-UHFFFAOYSA-N

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2-(Bromoacetyl)thiophene is a chemical compound widely used in organic synthesis reactions, particularly in the development of complex heterocyclic compounds. This compound is derived from the thiophene ring, which is modified with a bromoacetyl group, making it a valuable building block in synthetic chemistry. In laboratory settings, it serves as a key reagent for various synthetic processes, including substitution and coupling reactions. Its versatility allows it to be integrated into the synthesis of compounds with specific biological activities, making it a crucial component in research focused on pharmaceutical and material sciences.

The compound’s reactivity and stability under controlled conditions make it a preferred choice for chemists. Its ability to form stable intermediates and participate in multiple reaction pathways enhances its utility in synthetic routes. The presence of both bromo and acetyl functionalities provides multiple sites for further chemical modifications, enabling the creation of diverse molecular structures. These properties make it an essential tool for researchers aiming to develop new compounds with tailored properties.

In Indonesian laboratories, 2-(Bromoacetyl)thiophene is commonly used in organic chemistry research, especially in the synthesis of bioactive compounds and advanced materials. It is a key reagent in the development of pharmaceuticals and functional materials, supporting innovation in both academic and industrial research settings. Its role in creating complex molecular architectures underscores its importance in modern chemical research.

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactive thiophene core and bromoacetyl functionality.
Development of bioactive molecules for pharmaceutical research as it supports the formation of complex structures.
Coupling reactions where its functional groups enable efficient bond formation between different molecular entities.
Synthesis of advanced materials in material science due to its structural versatility and reactivity.
Research into new chemical entities for drug discovery as it provides a flexible platform for molecular modification.

Brand	TCI
CAS number	10531-41-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid (as per standard product description)
Storage	Store in a cool, dry place away from light and incompatible substances

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its stability. Due to its reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to minimize direct contact. It is important to ensure that it is kept separate from incompatible materials to avoid chemical interactions. Proper labeling of storage containers is essential for safe handling and to prevent accidental exposure in a laboratory setting.

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